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Medical Coverage Policy Non-invasive Measurement of Left Ventricular End Diastolic Pressure (LVEDP) in the Outpatient Setting Device/Equipment Effective Date: Drug Medical 3/3/2009 Surgery Policy Last Updated: Test Other 4/5/2011 Prospective review is recommended/required. Please check the member agreement for preauthorization guidelines. Prospective review is not required. Description: Left ventricular end diastolic pressure (LVEDP), the pressure at the end of the filling phase of the heart, is elevated in congestive heart failure. Its measurement may be useful in the management of patients with congestive heart failure. Non-invasive measurements of LVEDP have been developed based on the observation that the arterial pressure during the strain phase of the Valsalva maneuver may directly reflect the LVEDP. For example, arterial pressure response during the Valsalva maneuver generally shows 4 distinct phases, which can be recorded and analyzed. The VeriCor device (CVP Diagnostics, Boston, MA) is an example of a device for the non-invasive measurement of LVEDP that has received U.S. Food and Drug Administration (FDA) clearance through the 510(k) process. The VeriCor device consists of a digital expiratory manometer coupled with a continuous arterial pressure monitor and a medical grade computer. A tonometric sensor is attached to the patient’s wrist with a blood pressure cuff attached to the arm. After an 8-minute tonometric calibration period is completed, the VeriCor system is ready for use. For the test, the patient is prompted to perform a Valsalva maneuver by blowing into the mouthpiece of the digital monometer to produce an expiratory pressure of 20 to 30 mmHg for a minimum of 8 seconds. The digital signals are collected and stored on a medical grade computer. The arterial pressure signals are then analyzed according to algorithms that were developed to most accurately predict pulmonary capillary wedge pressure. Medical Criteria: Not applicable. Policy: Non-invasive measurement of left ventricular end diastolic pressure (LVEDP) in the outpatient setting is considered not medically necessary because there is insufficient evidence in the published medical literature to demonstrate its efficacy. Coverage: Benefits may vary between groups and contracts. Please refer to the appropriate Evidence of Coverage, Subscriber Agreement contract for the applicable Services Not Medically Necessary benefits/coverage. Coding: Providers should file left ventricular filling pressure indirect measurement by computerized calibration of the arterial waveform response to Valsalva maneuver using the following unlisted code: 93799 Also known as: Congestive Heart Failure Left Ventricular End Diastolic Pressure Non-invasive Measurement LVEDP Non-invasive Measurement VeriCor Publications: Provider Update, May 2009 Provider Update, Jun 2010 Provider Update, May 2011 This medical policy is made available to you for informational purposes only. It is not a guarantee of payment or a substitute for your medical judgment in the treatment of your patients. Benefits and eligibility are determined by the member's subscriber agreement or member certificate and/or the employer agreement, and those documents will supersede the provisions of this medical policy. For information on member-specific benefits, call the provider call center. If you provide services to a member which are determined to not be medically necessary (or in some cases medically necessary services which are non-covered benefits), you may not charge the member for the services unless you have informed the member and they have agreed in writing in advance to continue with the treatment at their own expense. Please refer to your participation agreement(s) for the applicable provisions. This policy is current at the time of publication; however, medical practices, technology, and knowledge are constantly changing. BCBSRI reserves the right to review and revise this policy for any reason and at any time, with or without notice.